A3B and ABAB aminophthalocyanines: Building blocks for dimeric and polymeric constructs

Safiye Bozkurt Ekren, F. Dumoulin, E. Musluoǧlu, V. Ahsen, Ö. Güngör
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引用次数: 2

Abstract

Mono or diamino phthalocyanines with A3B or crosswise ABAB substitution patterns have been synthesized and used as building blocks for the preparation of dimeric and polymeric phthalocyanines. For this, 4,5-di(dodecylsulfanyl) phthalonitrile was converted into 1,3-diimino-6,7-di-([Formula: see text]-dodecylsulfanyl)-isoiminoindoline and then reacted with 6-nitro-1,3,3-trichloroisoindoline. The nitro functions on the resulting inseparable mixture of A3B and ABAB phthalocyanines were reduced into amines by Na2S and the phthalocyanines could be chromatographically separated. Dimeric phthalocyanine was synthesized by the reaction of the mono-amino AB3 with sebacoyldichloride, and a poorly soluble linear polymeric material was obtained by reaction of the ABAB di-amino phthalocyanine with sebacoyl dichloride.
A3B和ABAB氨基酞菁:二聚体和聚合物结构的构建块
已经合成了具有A3B或横向ABAB取代模式的单或二氨基酞菁,并将其用作制备二聚体和聚合物酞菁的基本单元。为此,4,5-二(十二烷基磺酰)邻苯二腈被转化为1,3-二亚胺-6,7-二([公式:见原文]-十二烷基磺酰)-异亚胺吲哚,然后与6-硝基-1,3,3-三氯异吲哚反应。得到的A3B和ABAB酞菁不可分离的混合物上的硝基功能被Na2S还原成胺,可以色谱分离酞菁。以单氨基AB3与皮脂酰二氯反应合成二聚体酞菁,并以ABAB二氨基酞菁与皮脂酰二氯反应得到难溶的线状高分子材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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